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T2435EPZ011989
EPZ011989 is a effective, specific orally bioavailable EZH2 inhibitor with Ki < 3 nM for EZH2 Y646 and EZH2 wt; 15-fold selectivity over EZH1 and >3000-fold selectivity over other HMTase.
价 格：￥电议型 号：T2435产 地：中国大陆
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T24214PhenamacrilJS399 19；JS39919；苯那普利
JS399-19 is acyanoacrylate fungicide, has powerful inhibition against Fusarium species, especially to Fusarium graminearum. JS399-19 is a specific Fusarium myosin I inhibitor.
价 格：￥电议型 号：T24214产 地：中国大陆
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T2419BMS-794833BMS794833
BMS-794833 is a potent ATP competitive inhibitor of Met/VEGFR2; a prodrug of BMS-817378.
价 格：￥电议型 号：T2419产 地：中国大陆
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T2385IpragliflozinASP1941；伊格列净
Ipragliflozin is under investigation in Type 2 Diabetes and Diabetes Mellitus, Type 2.
价 格：￥电议型 号：T2385产 地：中国大陆
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T2381AbemaciclibLY2835219；CDK4/6 dual inhibitor
LY2835219 is an effective and specific CDK4/6 inhibitor (IC50: 2/10 nM).
价 格：￥电议型 号：T2381产 地：中国大陆
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T2369RociletinibAVL-301；CNX-419；CO-1686
Rociletinib is an orally available small molecule, irreversible inhibitor of epidermal growth factor receptor (EGFR) with potential antineoplastic activity.
价 格：￥电议型 号：T2369产 地：中国大陆
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T2338JZL195
JZL195 is a selective and efficacious dual FAAH/MAGL inhibitor.
价 格：￥电议型 号：T2338产 地：中国大陆
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T2319Acotiamide monohydrochloride trihydrateYM-443 HCl；Z-338 HCl；Acotiamide hydrochloride；盐酸阿考替胺
Acotiamide Hydrochloride is the hydrochloride salt form of acotiamide, a prokinetic agent with gastrointestinal (GI) motility-enhancing activity. Although the exact mechanism by which acotiamide exerts its effect has yet to be fully elucidated, this agent
价 格：￥电议型 号：T2319产 地：中国大陆
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T2301SB 202190FHPI；SB202190
SB 202190 is a selective and cell-permeable inhibitor of p38 MAPK (IC50s: 50/100 nM for p38α/p38β).
价 格：￥电议型 号：T2301产 地：中国大陆
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T22996ML-191
ML-191 is an inhibitor of LPI-induced phosphorylation of ERK1/2.
价 格：￥电议型 号：T22996产 地：中国大陆
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T22851ICI 63197三氮唑嘧啶酮；2-Amino-6-methyl-4-propyl-[1,2,4]triazolo[1,5-a]pyrimidin-5(4H)-one
ICI 63197 is a PDE4 inhibitor.
价 格：￥电议型 号：T22851产 地：中国大陆
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T22654Selfotel塞福太；CGS 19755；LY-272541
CGS 19755 is a selective, competitive NMDA antagonist that inhibits [3H]-3-(2-carboxypiperazin-4-yl)propyl-1-phosphonic acid binding to NMDA-type receptors with IC50 of 50 nM.
价 格：￥电议型 号：T22654产 地：中国大陆
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T22419S-Methylisothiourea sulfateS-甲基异硫脲硫酸盐；S-甲基异硫脲半硫酸盐；(S)-Methylisothiourea sulfate
S-Methylisothiourea sulfate is a potent and selective inhibitor of iNOS and exerts beneficial effects in rodent models of septic shock[1].
价 格：￥电议型 号：T22419产 地：中国大陆
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T22301L-838417 D9CTP354 (C-21191)；C-21191；CTP354
L-838417 is a novel deuterated subtype-selective GABAA positive allosteric modulator, acting as a partial agonist at α2, α3 and α5 subtypes[1].
价 格：￥电议型 号：T22301产 地：中国大陆
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T22195CBFβ Inhibitor5-乙基-4-(4-甲氧基苯基)-1,3-噻唑-2-胺；5-Ethyl-4-(4-methoxy-phenyl)-thiazol-2-ylamine
CBFβ Inhibitor is a cell-permeable CBFβ inhibitor and inhibits its association with Runx1.
价 格：￥电议型 号：T22195产 地：中国大陆
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T2219Puromycin dihydrochloride嘌呤霉素二盐酸盐水合物；嘌呤霉素二盐酸盐；CL13900 dihydrochloride；Puromycin 2HCl
Puromycin hydrochloride is a cinnamamido ADENOSINE found in STREPTOMYCES alboniger. It inhibits protein synthesis by binding to RNA. It is an antineoplastic and antitrypanosomal agent and is used in research as an inhibitor of protein synthesis.
价 格：￥电议型 号：T2219产 地：中国大陆
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T22142RO8191CDM-3008；RO4948191
RO8191 (CDM-3008), an imidazonaphthyridine compound, is an agonist of interferon (IFN) receptor.
价 格：￥电议型 号：T22142产 地：中国大陆
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T22103ML-193ML193；CID 1261822
ML-193 is a potent and selective GPR55 antagonist( IC50 : 221 nM). It shows more than 27-fold selectivity for GPR55 over GPR35, CB1 and CB2, and can improve the motor and the sensorimotor deficits of Parkinson’s disease (PD) rats.
价 格：￥电议型 号：T22103产 地：中国大陆
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T22019ABT 724 trihydrochloride
ABT 724 trihydrochloride is an effective and selective agonist of the D4 receptor (EC50 = 12.4 nM, 14.3 nM, and 23.2 nM for human, rat and ferret, respectively). ABT-724 trihydrochloride can be used in erectile dysfunction studies.
价 格：￥电议型 号：T22019产 地：中国大陆
